ENST00000609686.4:c.-18-119G>C
MANE Select
|
ENSP00000477455.1:n.-18-119G>C
|
|
ENST00000630791.2:c.-18-119G>C
|
ENSP00000486677.2:n.-18-119G>C
|
|
ENST00000609686.3:c.-18-119G>C
|
ENSP00000477455.1:n.-18-119G>C
|
|
ENST00000627535.2:c.-18-119G>C
|
ENSP00000486411.1:n.-18-119G>C
|
|
ENST00000630791.1:c.-18-119G>C
|
ENSP00000486677.1:n.-18-119G>C
|
|
NM_000834.3:c.-18-119G>C
|
NP_000825.2:n.-18-119G>C
|
|
XM_011520628.1:c.-18-119G>C
|
XP_011518930.1:n.-18-119G>C
|
|
XM_011520629.1:c.-18-119G>C
|
XP_011518931.1:n.-18-119G>C
|
|
XM_011520630.1:c.-18-119G>C
|
XP_011518932.1:n.-18-119G>C
|
|
NM_000834.4:c.-18-119G>C
|
NP_000825.2:n.-18-119G>C
|
|
XM_011520628.2:c.-18-119G>C
|
XP_011518930.1:n.-18-119G>C
|
|
XM_011520629.2:c.-18-119G>C
|
XP_011518931.1:n.-18-119G>C
|
|
XM_017019219.2:c.-18-119G>C
|
XP_016874708.1:n.-18-119G>C
|
|
NM_000834.5:c.-18-119G>C
MANE Select
|
NP_000825.2:n.-18-119G>C
|
|